Variant report

Variant	nsv879861
Chromosome Location	chr4:122126808-122181277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:122173409-122173695	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:122173315-122173607	K562	blood:	n/a	n/a
3	ATF2	chr4:122177321-122178024	GM12878	blood:	n/a	n/a
4	ATF2	chr4:122148396-122148959	GM12878	blood:	n/a	n/a
5	ATF2	chr4:122177356-122178080	GM12878	blood:	n/a	n/a
6	BATF	chr4:122164564-122164885	GM12878	blood:	n/a	n/a
7	BATF	chr4:122177453-122177933	GM12878	blood:	n/a	n/a
8	BATF	chr4:122177428-122177980	GM12878	blood:	n/a	chr4:122177927-122177937
9	BCL11A	chr4:122177494-122177812	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:122177450-122177954	GM12878	blood:	n/a	chr4:122177929-122177938
11	BCL3	chr4:122177526-122177897	GM12878	blood:	n/a	n/a
12	BCL3	chr4:122177449-122177887	GM12878	blood:	n/a	n/a
13	BCLAF1	chr4:122177378-122178097	GM12878	blood:	n/a	chr4:122177929-122177938
14	BHLHE40	chr4:122143519-122143557	GM12878	blood:	n/a	n/a
15	CEBPB	chr4:122177571-122177874	IMR90	lung:	n/a	chr4:122177596-122177609
16	CEBPB	chr4:122138620-122138977	Hela-S3	cervix:	n/a	chr4:122138807-122138818 chr4:122138807-122138816 chr4:122138805-122138818 chr4:122138805-122138818 chr4:122138763-122138776 chr4:122138805-122138816 chr4:122138765-122138776
17	CEBPB	chr4:122138690-122139000	HepG2	liver:	n/a	chr4:122138807-122138818 chr4:122138807-122138816 chr4:122138805-122138818 chr4:122138805-122138818 chr4:122138763-122138776 chr4:122138805-122138816 chr4:122138765-122138776
18	CEBPB	chr4:122175015-122175270	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:122138714-122138929	A549	lung:	n/a	chr4:122138807-122138818 chr4:122138807-122138816 chr4:122138805-122138818 chr4:122138805-122138818 chr4:122138763-122138776 chr4:122138805-122138816 chr4:122138765-122138776
20	CEBPB	chr4:122177418-122178075	HCT-116	colon:	n/a	chr4:122177596-122177609
21	CEBPB	chr4:122138629-122138989	IMR90	lung:	n/a	chr4:122138807-122138818 chr4:122138807-122138816 chr4:122138805-122138818 chr4:122138805-122138818 chr4:122138763-122138776 chr4:122138805-122138816 chr4:122138765-122138776
22	CEBPB	chr4:122177518-122177933	Hela-S3	cervix:	n/a	chr4:122177596-122177609
23	CEBPB	chr4:122177408-122178065	GM12878	blood:	n/a	chr4:122177596-122177609
24	CREB1	chr4:122177470-122177970	GM12878	blood:	n/a	n/a
25	CTCF	chr4:122148780-122148930	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr4:122148660-122148810	HMF	breast:	n/a	n/a
27	CTCF	chr4:122172659-122172684	Lung_OC	lung:	n/a	n/a
28	CTCF	chr4:122148880-122149030	RPTEC	kidney:	n/a	n/a
29	CTCF	chr4:122173500-122173650	NHEK	skin:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
30	CTCF	chr4:122173402-122173704	HepG2	liver:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
31	CTCF	chr4:122173500-122173650	GM12801	blood:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
32	CTCF	chr4:122173440-122173590	HAc	cerebellar:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
33	CTCF	chr4:122173500-122173650	RPTEC	kidney:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
34	CTCF	chr4:122172980-122173130	GM12873	blood:	n/a	n/a
35	CTCF	chr4:122173460-122173610	GM12871	blood:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
36	CTCF	chr4:122173481-122173665	GM20000	blood:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
37	CTCF	chr4:122148760-122148910	GM12865	blood:	n/a	n/a
38	CTCF	chr4:122173005-122173075	GM10248	blood:	n/a	n/a
39	CTCF	chr4:122148860-122149010	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr4:122148780-122148930	GM12873	blood:	n/a	n/a
41	CTCF	chr4:122173500-122173650	GM12874	blood:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
42	CTCF	chr4:122173352-122173726	A549	lung:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
43	CTCF	chr4:122173500-122173650	HCT-116	colon:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
44	CTCF	chr4:122148800-122148950	AG04450	lung:	n/a	n/a
45	CTCF	chr4:122148760-122148910	GM12870	blood:	n/a	n/a
46	CTCF	chr4:122173480-122173630	SAEC	small airway:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
47	CTCF	chr4:122173500-122173650	NHLF	lung:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
48	CTCF	chr4:122148710-122148959	GM12878	blood:	n/a	n/a
49	CTCF	chr4:122173203-122173804	A549	lung:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576
50	CTCF	chr4:122173500-122173650	HA-sp	spinal cord:	n/a	chr4:122173559-122173575 chr4:122173561-122173571 chr4:122173564-122173573 chr4:122173562-122173583 chr4:122173563-122173576 chr4:122173560-122173578 chr4:122173553-122173574 chr4:122173560-122173573 chr4:122173558-122173576

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:122159665-122159715	NT2-D1	testis:	n/a
2	chr4:122155606-122155656	SAEC	small airway:	n/a
3	chr4:122137696-122137746	AoSMC	blood vessel:	n/a
4	chr4:122137696-122137746	HRCEpiC	kidney:	n/a
5	chr4:122137696-122137746	SKMC	muscle:	n/a
6	chr4:122155606-122155656	SK-N-SH_RA	brain:	n/a
7	chr4:122137696-122137746	GM06990	blood:	n/a
8	chr4:122138632-122138682	BE2_C	brain:	n/a
9	chr4:122137613-122137663	Hepatocyte	liver:	n/a
10	chr4:122155606-122155656	U87	brain:	n/a
11	chr4:122155606-122155656	GM12891	blood:	n/a
12	chr4:122138632-122138682	IMR90	lung:	fetal
13	chr4:122155606-122155656	AG04449	skin:	fetal
14	chr4:122159665-122159715	HepG2	liver:	n/a
15	chr4:122137696-122137746	BJ	skin:	n/a
16	chr4:122155606-122155656	HEEpiC	esophagus:	n/a
17	chr4:122159665-122159715	HCF	heart:	n/a
18	chr4:122137696-122137746	T-47D	breast:	n/a
19	chr4:122159665-122159715	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:122137696-122137746	CMK	blood:	n/a
21	chr4:122155606-122155656	GM12878	blood:	n/a
22	chr4:122159665-122159715	K562	blood:	n/a
23	chr4:122159665-122159715	Caco-2	colon:	n/a
24	chr4:122137696-122137746	HCT-116	colon:	n/a
25	chr4:122137613-122137663	SAEC	small airway:	n/a
26	chr4:122155606-122155656	HEK293	kidney:	embryo
27	chr4:122137696-122137746	Caco-2	colon:	n/a
28	chr4:122137696-122137746	HL-60	blood:	n/a
29	chr4:122159665-122159715	LNCaP	prostate:	n/a
30	chr4:122155606-122155656	ECC-1	luminal epithelium:	n/a
31	chr4:122155606-122155656	A549	lung:	n/a
32	chr4:122137613-122137663	SKMC	muscle:	n/a
33	chr4:122137613-122137663	NH-A	brain:	n/a
34	chr4:122138632-122138682	GM06990	blood:	n/a
35	chr4:122138632-122138682	NT2-D1	testis:	n/a
36	chr4:122138632-122138682	ECC-1	luminal epithelium:	n/a
37	chr4:122159665-122159715	PrEC	prostate:	n/a
38	chr4:122155606-122155656	Caco-2	colon:	n/a
39	chr4:122155606-122155656	IMR90	lung:	fetal
40	chr4:122137613-122137663	AG09309	skin:	n/a
41	chr4:122159665-122159715	HCPEpiC	choroid plexus:	n/a
42	chr4:122159665-122159715	AG09319	gingival:	n/a
43	chr4:122137696-122137746	PANC-1	pancreas:	n/a
44	chr4:122137613-122137663	NB4	blood:	n/a
45	chr4:122155606-122155656	NH-A	brain:	n/a
46	chr4:122138632-122138682	NB4	blood:	n/a
47	chr4:122155606-122155656	NT2-D1	testis:	n/a
48	chr4:122155606-122155656	HCF	heart:	n/a
49	chr4:122137696-122137746	RPTEC	kidney:	n/a
50	chr4:122155606-122155656	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:122113432..122114180-chr4:122173027..122174043,3	MCF-7	breast:
2	chr4:122179294..122180851-chr4:122194638..122196291,2	MCF-7	breast:
3	chr4:122138311..122140840-chr4:122141351..122144683,3	K562	blood:
4	chr4:122138311..122140840-chr4:122141351..122144683,3	K562	blood:
5	chr4:122132988..122135526-chr4:122137849..122140613,2	K562	blood:
6	chr4:122113302..122114320-chr4:122173099..122174082,9	MCF-7	breast:
7	chr4:122132988..122135526-chr4:122137849..122140613,2	K562	blood:
8	chr4:122146897..122149532-chr4:122150915..122153433,2	MCF-7	breast:
9	chr4:122135869..122137614-chr4:122143872..122146704,2	MCF-7	breast:
10	chr1:11969686..11970281-chr4:122155842..122156342,2	Hela-S3	cervix:
11	chr4:122135869..122137614-chr4:122143872..122146704,2	MCF-7	breast:
12	chr4:122113303..122113806-chr4:122173095..122173613,2	K562	blood:
13	chr4:122120724..122123335-chr4:122133956..122135681,2	MCF-7	breast:

Variant related genes	Relation type
TNIP3	TF binding region
TNIP3	CpG island
ENSG00000050730	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000252183	chromatin interactions

Extended variants
information (count: 2070 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2070 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13116936	chr4:122126808-122126809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs189748997	chr4:122126823-122126824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560927189	chr4:122126833-122126834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559099784	chr4:122126888-122126889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192976663	chr4:122126927-122126928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185257950	chr4:122126934-122126935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569928333	chr4:122126936-122126937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545348529	chr4:122126998-122126999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538825982	chr4:122127001-122127002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552847409	chr4:122127029-122127030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35581258	chr4:122127047-122127048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139835461	chr4:122127077-122127078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531110000	chr4:122127084-122127085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535303930	chr4:122127087-122127088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112261069	chr4:122127107-122127108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150019142	chr4:122127134-122127135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574474886	chr4:122127135-122127136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565349608	chr4:122127142-122127143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144275915	chr4:122127165-122127166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377297729	chr4:122127205-122127206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190579705	chr4:122127221-122127222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530577518	chr4:122127227-122127228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545645488	chr4:122127249-122127250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148468467	chr4:122127295-122127296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142613505	chr4:122127338-122127339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181938056	chr4:122127381-122127382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186307960	chr4:122127479-122127480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188351743	chr4:122127510-122127511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116659035	chr4:122127532-122127533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563594590	chr4:122127540-122127541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532621182	chr4:122127591-122127592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552523165	chr4:122127606-122127607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548715662	chr4:122127652-122127653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140121953	chr4:122127693-122127694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61344205	chr4:122127704-122127705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74496564	chr4:122127705-122127706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566257673	chr4:122127730-122127731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs180762019	chr4:122127821-122127822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548858600	chr4:122127882-122127883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186481130	chr4:122127949-122127950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537016408	chr4:122127963-122127964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557109791	chr4:122127970-122127971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150970817	chr4:122127990-122127991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113478329	chr4:122128060-122128061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371745145	chr4:122128094-122128095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572986842	chr4:122128137-122128138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541734374	chr4:122128163-122128164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141132976	chr4:122128190-122128191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574505071	chr4:122128195-122128196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561808590	chr4:122128209-122128210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122122200-122137600	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr4:122129400-122130800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr4:122129800-122130800	Enhancers	Hela-S3	cervix
4	chr4:122130800-122137600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr4:122133800-122134200	Enhancers	Fetal Lung	lung
6	chr4:122134200-122134800	Enhancers	NHDF-Ad	bronchial
7	chr4:122134200-122136600	Weak transcription	Fetal Lung	lung
8	chr4:122134800-122135200	Weak transcription	NHDF-Ad	bronchial
9	chr4:122135200-122135400	Enhancers	NHDF-Ad	bronchial
10	chr4:122135200-122135800	Enhancers	Primary T cells fromperipheralblood	blood
11	chr4:122135200-122135800	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr4:122135400-122137600	Weak transcription	NHDF-Ad	bronchial
13	chr4:122135800-122136000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr4:122135800-122137800	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr4:122136000-122136400	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr4:122136400-122137200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr4:122136600-122143200	Enhancers	Fetal Lung	lung
18	chr4:122136800-122138800	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr4:122137200-122138800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr4:122137200-122140800	Enhancers	Fetal Stomach	stomach
21	chr4:122137400-122138400	Enhancers	Primary T cells from cord blood	blood
22	chr4:122137600-122138000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
23	chr4:122137600-122138400	Enhancers	Placenta Amnion	Placenta Amnion
24	chr4:122137600-122139600	Enhancers	NHDF-Ad	bronchial
25	chr4:122137800-122138200	Enhancers	Primary T cells fromperipheralblood	blood
26	chr4:122137800-122138600	Enhancers	Fetal Muscle Leg	muscle
27	chr4:122137800-122140400	Enhancers	NHLF	lung
28	chr4:122138000-122138200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr4:122138000-122138800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
30	chr4:122138200-122139600	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr4:122138200-122141800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr4:122138400-122138800	Enhancers	Placenta	Placenta
33	chr4:122138400-122141600	Weak transcription	Primary T cells from cord blood	blood
34	chr4:122138600-122138800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:122138600-122139200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:122138600-122139800	Weak transcription	Fetal Muscle Leg	muscle
37	chr4:122138800-122139200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr4:122138800-122139600	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr4:122138800-122140800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr4:122138800-122141400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr4:122138800-122147600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:122139200-122140400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:122139600-122140000	Enhancers	Primary T cells fromperipheralblood	blood
44	chr4:122139600-122142600	Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr4:122139800-122140600	Enhancers	Fetal Muscle Leg	muscle
46	chr4:122140000-122141800	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr4:122140400-122140600	Flanking Active TSS	NHLF	lung
48	chr4:122140400-122140800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:122140400-122140800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:122140600-122140800	Active TSS	NHLF	lung

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