Variant report

Variant	nsv428799
Chromosome Location	chr11:4186981-4336490
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1229)
CpG islands
(count:733)
Chromatin interactive
region (count:25)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4205750-4205950	K562	blood:	n/a	n/a
2	ARID3A	chr11:4203458-4203639	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:4216109-4216597	K562	blood:	n/a	n/a
4	ARID3A	chr11:4208203-4208403	K562	blood:	n/a	n/a
5	ATF1	chr11:4218126-4218315	K562	blood:	n/a	n/a
6	ATF1	chr11:4216207-4216475	K562	blood:	n/a	n/a
7	ATF3	chr11:4208748-4209028	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:4208789-4209061	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:4233294-4233648	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:4209051-4209129	K562	blood:	n/a	n/a
11	BACH1	chr11:4224962-4225178	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr11:4202929-4203828	K562	blood:	n/a	n/a
13	BHLHE40	chr11:4208122-4208459	K562	blood:	n/a	n/a
14	BHLHE40	chr11:4208769-4209074	GM12878	blood:	n/a	chr11:4208989-4209005
15	BHLHE40	chr11:4208773-4209110	K562	blood:	n/a	chr11:4208989-4209005
16	BHLHE40	chr11:4216191-4216537	K562	blood:	n/a	n/a
17	BRCA1	chr11:4208855-4208989	HepG2	liver:	n/a	n/a
18	BRCA1	chr11:4208834-4209055	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr11:4208772-4209129	K562	blood:	n/a	n/a
20	CBX3	chr11:4208019-4208474	K562	blood:	n/a	n/a
21	CBX3	chr11:4207969-4208291	K562	blood:	n/a	n/a
22	CBX3	chr11:4203292-4203924	K562	blood:	n/a	n/a
23	CCNT2	chr11:4216171-4216526	K562	blood:	n/a	n/a
24	CCNT2	chr11:4208203-4209367	K562	blood:	n/a	chr11:4209066-4209075 chr11:4208444-4208453
25	CCNT2	chr11:4205703-4206232	K562	blood:	n/a	n/a
26	CEBPB	chr11:4232604-4232820	IMR90	lung:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
27	CEBPB	chr11:4232611-4232857	HepG2	liver:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
28	CEBPB	chr11:4205574-4206017	K562	blood:	n/a	chr11:4205745-4205756
29	CEBPB	chr11:4208855-4209254	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr11:4208893-4208908	K562	blood:	n/a	n/a
31	CEBPB	chr11:4233297-4233351	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr11:4208794-4209159	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:4228834-4228864	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr11:4205582-4205901	H1-hESC	embryonic stem cell:	n/a	chr11:4205745-4205756
35	CEBPB	chr11:4257961-4258189	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
36	CEBPB	chr11:4205560-4205942	IMR90	lung:	n/a	chr11:4205745-4205756
37	CEBPB	chr11:4205568-4205916	Hela-S3	cervix:	n/a	chr11:4205745-4205756
38	CEBPB	chr11:4220020-4220204	K562	blood:	n/a	n/a
39	CEBPB	chr11:4257965-4258134	K562	blood:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
40	CEBPB	chr11:4208020-4208479	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:4205574-4205936	A549	lung:	n/a	chr11:4205745-4205756
42	CEBPB	chr11:4224768-4225111	K562	blood:	n/a	n/a
43	CEBPB	chr11:4205634-4205851	K562	blood:	n/a	chr11:4205745-4205756
44	CEBPB	chr11:4205566-4205944	HepG2	liver:	n/a	chr11:4205745-4205756
45	CEBPB	chr11:4257958-4258231	HepG2	liver:	n/a	chr11:4258101-4258112 chr11:4258101-4258110 chr11:4258099-4258110
46	CEBPB	chr11:4208295-4208391	K562	blood:	n/a	n/a
47	CEBPB	chr11:4216252-4216447	K562	blood:	n/a	n/a
48	CEBPB	chr11:4232578-4232904	K562	blood:	n/a	chr11:4232731-4232742 chr11:4232731-4232744 chr11:4232732-4232743 chr11:4232697-4232708
49	CEBPD	chr11:4216035-4216623	K562	blood:	n/a	n/a
50	CEBPD	chr11:4216067-4216617	K562	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4206098-4206148	AoSMC	blood vessel:	n/a
2	chr11:4206098-4206148	AoSMC	blood vessel:	n/a
3	chr11:4208278-4208328	SK-N-MC	brain:	n/a
4	chr11:4208449-4208499	HUVEC	blood vessel:	n/a
5	chr11:4208905-4208955	LNCaP	prostate:	n/a
6	chr11:4208905-4208955	Caco-2	colon:	n/a
7	chr11:4259129-4259179	HNPCEpiC	eye:	n/a
8	chr11:4209397-4209447	SK-N-SH_RA	brain:	n/a
9	chr11:4208905-4208955	MCF10A-Er-Src	breast:	n/a
10	chr11:4209397-4209447	U87	brain:	n/a
11	chr11:4212446-4212496	HL-60	blood:	n/a
12	chr11:4212446-4212496	H1-hESC	embryonic stem cell:	embryo
13	chr11:4206098-4206148	MCF10A-Er-Src	breast:	n/a
14	chr11:4209397-4209447	Hela-S3	cervix:	n/a
15	chr11:4212446-4212496	IMR90	lung:	fetal
16	chr11:4206098-4206148	HCF	heart:	n/a
17	chr11:4208723-4208773	MCF10A-Er-Src	breast:	n/a
18	chr11:4233502-4233552	HepG2	liver:	n/a
19	chr11:4212446-4212496	GM12892	blood:	n/a
20	chr11:4209120-4209170	Hepatocyte	liver:	n/a
21	chr11:4258933-4258983	Hela-S3	cervix:	n/a
22	chr11:4259129-4259179	GM06990	blood:	n/a
23	chr11:4208723-4208773	SKMC	muscle:	n/a
24	chr11:4258933-4258983	NHBE	bronchial:	n/a
25	chr11:4206098-4206148	Jurkat	blood:	n/a
26	chr11:4259129-4259179	HCF	heart:	n/a
27	chr11:4208278-4208328	Caco-2	colon:	n/a
28	chr11:4212471-4212521	AoSMC	blood vessel:	n/a
29	chr11:4233502-4233552	ECC-1	luminal epithelium:	n/a
30	chr11:4208278-4208328	HAEpiC	amniotic membrane:	n/a
31	chr11:4208449-4208499	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:4233502-4233552	NHBE	bronchial:	n/a
33	chr11:4209120-4209170	MCF-7	breast:	n/a
34	chr11:4208905-4208955	ovcar-3	ovarian:	n/a
35	chr11:4258933-4258983	AoSMC	blood vessel:	n/a
36	chr11:4209397-4209447	HRPEpiC	eye:	n/a
37	chr11:4212446-4212496	HCT-116	colon:	n/a
38	chr11:4209120-4209170	PrEC	prostate:	n/a
39	chr11:4209120-4209170	SK-N-SH	brain:	n/a
40	chr11:4208449-4208499	GM19239	blood:	n/a
41	chr11:4208449-4208499	T-47D	breast:	n/a
42	chr11:4208723-4208773	AG09319	gingival:	n/a
43	chr11:4208278-4208328	HCPEpiC	choroid plexus:	n/a
44	chr11:4259129-4259179	HEEpiC	esophagus:	n/a
45	chr11:4209120-4209170	AG04450	lung:	fetal
46	chr11:4258933-4258983	GM06990	blood:	n/a
47	chr11:4258933-4258983	AG10803	skin:	n/a
48	chr11:4212471-4212521	SAEC	small airway:	n/a
49	chr11:4212446-4212496	CMK	blood:	n/a
50	chr11:4259129-4259179	ProgFib	skin:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4208460..4209382-chr11:4513705..4515541,8	MCF-7	breast:
2	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
3	chr11:4184965..4186583-chr11:4189758..4191938,2	K562	blood:
4	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
5	chr11:4208515..4209433-chr11:4658248..4659042,2	K562	blood:
6	chr11:4205317..4208248-chr11:4208372..4210447,2	K562	blood:
7	chr11:4184965..4187541-chr11:4189558..4191938,3	K562	blood:
8	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
9	chr11:4208891..4209471-chr11:4572771..4573597,3	MCF-7	breast:
10	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
11	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
12	chr11:4115681..4117881-chr11:4185154..4187618,2	K562	blood:
13	chr11:4212714..4216366-chr11:4216449..4218991,4	K562	blood:
14	chr11:4201110..4205265-chr11:4206798..4209054,5	K562	blood:
15	chr11:4184965..4187541-chr11:4189558..4191938,3	K562	blood:
16	chr11:4198544..4201486-chr11:4213764..4216577,2	K562	blood:
17	chr11:4213864..4216366-chr11:4216449..4218991,2	K562	blood:
18	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:
19	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
20	chr11:4202964..4204119-chr11:4560777..4561880,3	MCF-7	breast:
21	chr11:4204877..4207550-chr11:4212628..4215055,2	K562	blood:
22	chr11:4199192..4201604-chr11:4201999..4204007,2	K562	blood:
23	chr11:4208647..4209327-chr11:4572350..4573087,2	MCF-7	breast:
24	chr11:4228086..4230506-chr11:4230807..4233604,2	K562	blood:
25	chr11:4216149..4218781-chr11:4227899..4229558,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR52B4-3	chr11:4201787-4201939	NONHSAT017641
2	lnc-OR52B4-3	chr11:4223487-4223875	NONHSAT017641
3	lnc-RRM1-2	chr11:4223489-4223883	NR_047550
4	lnc-RRM1-2	chr11:4201859-4201941	NONHSAT017642
5	lnc-RRM1-2	chr11:4201862-4201941	NONHSAT017640
6	lnc-RRM1-2	chr11:4208382-4208434	NR_047550
7	lnc-RRM1-2	chr11:4200829-4201124	NONHSAT017640
8	lnc-RRM1-2	chr11:4223489-4223875	NONHSAT017640
9	lnc-RRM1-2	chr11:4208370-4208434	ENSG00000254480.1
10	lnc-RRM1-2	chr11:4223489-4223881	NONHSAT017642
11	lnc-RRM1-2	chr11:4223489-4223885	ENSG00000254480.1

No data

Variant related genes	Relation type
ENSG00000255387	TF binding region
SSU72P5	TF binding region
SSU72P4	TF binding region
ENSG00000254480	TF binding region
SSU72P2	TF binding region
SSU72P6	TF binding region
ENSG00000255387	CpG island
SSU72P5	CpG island
SSU72P4	CpG island
ENSG00000254480	CpG island
SSU72P2	CpG island
SSU72P6	CpG island
ENSG00000254480	chromatin interactions
ENSG00000167325	chromatin interactions
ENSG00000255387	chromatin interactions

Extended variants
information (count: 2220 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2220 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75400439	chr11:4187000-4187001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs558291838	chr11:4187002-4187003	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs36063258	chr11:4187019-4187020	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs576727788	chr11:4187081-4187082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540778504	chr11:4187082-4187083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112955632	chr11:4187098-4187099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs386362184	chr11:4187099-4187100	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553144750	chr11:4187129-4187130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs546678746	chr11:4187132-4187133	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529820131	chr11:4187152-4187153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542076882	chr11:4187173-4187174	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2044135	chr11:4187233-4187234	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs138748836	chr11:4187261-4187262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs546048804	chr11:4187272-4187273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs11828628	chr11:4187282-4187283	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs112117114	chr11:4187372-4187373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs74912175	chr11:4187399-4187400	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547375026	chr11:4187451-4187452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs565881083	chr11:4187554-4187555	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184971924	chr11:4187566-4187567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116445898	chr11:4187651-4187652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570197061	chr11:4187656-4187657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537347858	chr11:4187678-4187679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559165507	chr11:4187691-4187692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571047676	chr11:4187721-4187722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534664121	chr11:4187722-4187723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs16929801	chr11:4187726-4187727	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs17284244	chr11:4187727-4187728	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs541915255	chr11:4187735-4187736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6578457	chr11:4187765-4187766	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs575348967	chr11:4187790-4187791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377383190	chr11:4187796-4187797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187487462	chr11:4187800-4187801	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs564442595	chr11:4187804-4187805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs528371072	chr11:4187814-4187815	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs541054881	chr11:4187819-4187820	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs559305585	chr11:4187861-4187862	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs370462102	chr11:4187927-4187928	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs367712845	chr11:4188027-4188028	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs530149442	chr11:4188058-4188059	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs192736479	chr11:4188089-4188090	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs570165145	chr11:4188092-4188093	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs531175475	chr11:4188178-4188179	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs374771912	chr11:4188184-4188185	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs1442727	chr11:4188188-4188189	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs372264644	chr11:4188243-4188244	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs184737559	chr11:4188291-4188292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs535323490	chr11:4188292-4188293	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs553021947	chr11:4188318-4188319	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs568036549	chr11:4188330-4188331	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4178800-4187800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:4187800-4190000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:4190000-4197000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:4196800-4197600	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr11:4196800-4197600	Active TSS	iPS-18 Cell Line	embryonic stem cell
6	chr11:4197000-4197400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:4197000-4197400	Active TSS	Placenta	Placenta
8	chr11:4197000-4197600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr11:4197000-4197600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:4197000-4197600	Active TSS	H9 Cell Line	embryonic stem cell
11	chr11:4197000-4197600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:4197000-4197600	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr11:4197000-4197600	Active TSS	HUES64 Cell Line	embryonic stem cell
14	chr11:4197000-4197600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:4197000-4197600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:4197000-4197600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr11:4197000-4197600	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr11:4197000-4197800	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr11:4197000-4197800	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr11:4197000-4197800	Active TSS	K562	blood
21	chr11:4197000-4198000	Active TSS	H1 Cell Line	embryonic stem cell
22	chr11:4197000-4198000	Active TSS	Duodenum Mucosa	Duodenum
23	chr11:4197400-4197800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:4197600-4197800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr11:4197600-4197800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr11:4197600-4198000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr11:4197600-4198200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
28	chr11:4197600-4208200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr11:4197600-4208200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:4197800-4198000	Flanking Active TSS	K562	blood
31	chr11:4198000-4198200	Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr11:4198000-4203000	Weak transcription	K562	blood
33	chr11:4200000-4208200	Enhancers	Liver	Liver
34	chr11:4200200-4200600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:4200600-4201000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:4201000-4201200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:4201200-4201800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:4201800-4202000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:4202200-4205400	Weak transcription	Fetal Heart	heart
40	chr11:4203000-4203400	Enhancers	Fetal Muscle Trunk	muscle
41	chr11:4203000-4203800	Enhancers	K562	blood
42	chr11:4203200-4203600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr11:4203800-4205400	Weak transcription	K562	blood
44	chr11:4205400-4206200	Enhancers	Right Ventricle	heart
45	chr11:4205400-4206400	Enhancers	Colon Smooth Muscle	Colon
46	chr11:4205400-4206400	Enhancers	K562	blood
47	chr11:4205400-4206800	Enhancers	Fetal Heart	heart
48	chr11:4205600-4205800	Enhancers	Fetal Lung	lung
49	chr11:4205600-4208000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr11:4205800-4206000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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