Variant report

Variant	esv2759423
Chromosome Location	chr6:44879791-45056758
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:971)
CpG islands
(count:61)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45011822-45012263	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:44934203-44935340	K562	blood:	n/a	n/a
3	ARID3A	chr6:44900932-44900942	K562	blood:	n/a	n/a
4	ARID3A	chr6:45017086-45017200	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:44928633-44929024	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:45017618-45017640	K562	blood:	n/a	n/a
7	ARID3A	chr6:44888556-44889970	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:44918920-44919276	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:44942228-44942585	K562	blood:	n/a	n/a
10	ARID3A	chr6:44907927-44908749	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:45025490-45025613	HepG2	liver:	n/a	n/a
12	ATF1	chr6:44888645-44888963	K562	blood:	n/a	n/a
13	ATF1	chr6:44934477-44934865	K562	blood:	n/a	n/a
14	ATF1	chr6:44893099-44893531	K562	blood:	n/a	n/a
15	ATF1	chr6:45025523-45025589	K562	blood:	n/a	n/a
16	ATF1	chr6:45016978-45017291	K562	blood:	n/a	n/a
17	ATF2	chr6:44966735-44967151	GM12878	blood:	n/a	n/a
18	ATF2	chr6:44966734-44967257	GM12878	blood:	n/a	n/a
19	ATF3	chr6:44934407-44934925	K562	blood:	n/a	n/a
20	BACH1	chr6:44965357-44965412	K562	blood:	n/a	n/a
21	BATF	chr6:44977334-44977648	GM12878	blood:	n/a	chr6:44977540-44977551
22	BATF	chr6:44977286-44977716	GM12878	blood:	n/a	chr6:44977540-44977551
23	BATF	chr6:44947204-44947474	GM12878	blood:	n/a	n/a
24	BATF	chr6:44966841-44967148	GM12878	blood:	n/a	n/a
25	BATF	chr6:44966783-44967196	GM12878	blood:	n/a	n/a
26	BCL3	chr6:44934546-44934913	K562	blood:	n/a	n/a
27	BHLHE40	chr6:44934500-44934832	K562	blood:	n/a	n/a
28	BHLHE40	chr6:45016926-45017297	K562	blood:	n/a	n/a
29	BHLHE40	chr6:44891304-44891474	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:44928669-44928955	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:44888678-44889228	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:44969459-44969727	GM12878	blood:	n/a	n/a
33	BRCA1	chr6:45011813-45011861	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr6:44934427-44934905	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:45016920-45017304	K562	blood:	n/a	n/a
36	CBX3	chr6:44934371-44934913	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:44940439-44940814	K562	blood:	n/a	n/a
38	CBX3	chr6:44940388-44940854	K562	blood:	n/a	n/a
39	CBX3	chr6:44889457-44889879	HCT-116	colon:	n/a	n/a
40	CBX3	chr6:44928552-44929041	HCT-116	colon:	n/a	n/a
41	CBX3	chr6:44934407-44934915	K562	blood:	n/a	n/a
42	CBX3	chr6:44934470-44934850	K562	blood:	n/a	n/a
43	CCNT2	chr6:44893177-44893452	K562	blood:	n/a	n/a
44	CCNT2	chr6:44934499-44934885	K562	blood:	n/a	n/a
45	CCNT2	chr6:45003117-45003383	K562	blood:	n/a	n/a
46	CCNT2	chr6:44888713-44888911	K562	blood:	n/a	chr6:44888832-44888852
47	CEBPB	chr6:44944620-44944869	HepG2	liver:	n/a	chr6:44944700-44944711
48	CEBPB	chr6:44971262-44971581	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:45042969-45043439	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:44963269-44963657	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45030454-45030504	HIPEpiC	eye:	n/a
2	chr6:45030454-45030504	MCF-7	breast:	n/a
3	chr6:45030454-45030504	HCF	heart:	n/a
4	chr6:45030454-45030504	Hela-S3	cervix:	n/a
5	chr6:45030454-45030504	NT2-D1	testis:	n/a
6	chr6:45030454-45030504	HepG2	liver:	n/a
7	chr6:45030454-45030504	AG04449	skin:	fetal
8	chr6:45030454-45030504	HNPCEpiC	eye:	n/a
9	chr6:45030454-45030504	Jurkat	blood:	n/a
10	chr6:45030454-45030504	LNCaP	prostate:	n/a
11	chr6:45030454-45030504	AoSMC	blood vessel:	n/a
12	chr6:45030454-45030504	HCT-116	colon:	n/a
13	chr6:45030454-45030504	BJ	skin:	n/a
14	chr6:45030454-45030504	SKMC	muscle:	n/a
15	chr6:45030454-45030504	IMR90	lung:	fetal
16	chr6:45030454-45030504	SK-N-SH	brain:	n/a
17	chr6:45030454-45030504	RPTEC	kidney:	n/a
18	chr6:45030454-45030504	HRCEpiC	kidney:	n/a
19	chr6:45030454-45030504	AG10803	skin:	n/a
20	chr6:45030454-45030504	HCM	heart:	n/a
21	chr6:45030454-45030504	H1-hESC	embryonic stem cell:	embryo
22	chr6:45030454-45030504	HEEpiC	esophagus:	n/a
23	chr6:45030454-45030504	AG09319	gingival:	n/a
24	chr6:45030454-45030504	HAEpiC	amniotic membrane:	n/a
25	chr6:45030454-45030504	AG04450	lung:	fetal
26	chr6:45030454-45030504	HRPEpiC	eye:	n/a
27	chr6:45030454-45030504	GM12891	blood:	n/a
28	chr6:45030454-45030504	GM12878	blood:	n/a
29	chr6:45030454-45030504	K562	blood:	n/a
30	chr6:45030454-45030504	ECC-1	luminal epithelium:	n/a
31	chr6:45030454-45030504	GM06990	blood:	n/a
32	chr6:45030454-45030504	NH-A	brain:	n/a
33	chr6:45030454-45030504	HL-60	blood:	n/a
34	chr6:45030454-45030504	HCPEpiC	choroid plexus:	n/a
35	chr6:45030454-45030504	SAEC	small airway:	n/a
36	chr6:45030454-45030504	PANC-1	pancreas:	n/a
37	chr6:45030454-45030504	GM12892	blood:	n/a
38	chr6:45030454-45030504	ovcar-3	ovarian:	n/a
39	chr6:45030454-45030504	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:45030454-45030504	CMK	blood:	n/a
41	chr6:45030454-45030504	U87	brain:	n/a
42	chr6:45030454-45030504	NHBE	bronchial:	n/a
43	chr6:45030454-45030504	GM19239	blood:	n/a
44	chr6:45030454-45030504	T-47D	breast:	n/a
45	chr6:45030454-45030504	NB4	blood:	n/a
46	chr6:45030454-45030504	SK-N-MC	brain:	n/a
47	chr6:45030454-45030504	HEK293	kidney:	embryo
48	chr6:45030454-45030504	HRE	kidney:	n/a
49	chr6:45030454-45030504	ProgFib	skin:	n/a
50	chr6:45030454-45030504	PFSK-1	brain:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:45054176..45055264-chr6:45386958..45387535,3	MCF-7	breast:
2	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
3	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
4	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
5	chr6:45008781..45011238-chr6:45015698..45018079,2	MCF-7	breast:
6	chr6:44996729..44999425-chr6:45119837..45121459,2	K562	blood:
7	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
8	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
9	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
10	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
11	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
12	chr6:45049112..45051418-chr6:45052257..45055062,3	K562	blood:
13	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
14	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
15	chr6:44874731..44877061-chr6:44885216..44887016,2	K562	blood:
16	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
17	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:
18	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:
19	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
20	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
21	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
22	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
23	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
24	chr6:44878819..44880569-chr6:44884458..44887437,2	MCF-7	breast:
25	chr6:45049112..45051418-chr6:45052257..45055062,3	K562	blood:
26	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
27	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
28	chr6:44443174..44444085-chr6:45053756..45054587,2	MCF-7	breast:
29	chr12:48357281..48357866-chr6:45012051..45012551,2	Hela-S3	cervix:
30	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
31	chr6:44878819..44880569-chr6:44884458..44887437,2	MCF-7	breast:
32	chr6:44888776..44891351-chr6:45344894..45347692,2	K562	blood:
33	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
34	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
35	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
36	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
37	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
38	chr6:45054220..45054815-chr6:45386791..45387562,3	MCF-7	breast:
39	chr6:45038976..45040613-chr6:45043879..45046271,2	K562	blood:
40	chr6:44928658..44930221-chr6:45326668..45328264,2	K562	blood:
41	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
42	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:

No data

Variant related genes	Relation type
SUPT3H	TF binding region
SUPT3H	CpG island
ENSG00000134291	chromatin interactions
ENSG00000196284	chromatin interactions

Extended variants
information (count: 6263 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:6263 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535505388	chr6:44879801-44879802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553809431	chr6:44879923-44879924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572067594	chr6:44879942-44879943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546120368	chr6:44879976-44879977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115269381	chr6:44879988-44879989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576215434	chr6:44879996-44879997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147064549	chr6:44880006-44880007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35534849	chr6:44880040-44880041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566218286	chr6:44880117-44880118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369301963	chr6:44880134-44880135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35979243	chr6:44880197-44880198	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs529349457	chr6:44880202-44880203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148100797	chr6:44880281-44880282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111400931	chr6:44880296-44880297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186777228	chr6:44880313-44880314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552077655	chr6:44880424-44880425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548590754	chr6:44880427-44880428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150624297	chr6:44880452-44880453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138701775	chr6:44880482-44880483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373068952	chr6:44880485-44880486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142711014	chr6:44880533-44880534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116410385	chr6:44880557-44880558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376818020	chr6:44880569-44880570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370886223	chr6:44880595-44880596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535591846	chr6:44880598-44880599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192870994	chr6:44880630-44880631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565714327	chr6:44880654-44880655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146028130	chr6:44880669-44880670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114175306	chr6:44880692-44880693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576266780	chr6:44880702-44880703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543654773	chr6:44880772-44880773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35692035	chr6:44880800-44880801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555189963	chr6:44880827-44880828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10948183	chr6:44880881-44880882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs373292959	chr6:44880888-44880889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559396457	chr6:44880905-44880906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6931343	chr6:44880937-44880938	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs113525662	chr6:44880953-44880954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563661659	chr6:44880968-44880969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs505772	chr6:44880986-44880987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs549695145	chr6:44881023-44881024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370165671	chr6:44881024-44881025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528683676	chr6:44881118-44881119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374924064	chr6:44881159-44881160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34172876	chr6:44881272-44881273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547545223	chr6:44881291-44881292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs28644430	chr6:44881294-44881295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565803765	chr6:44881330-44881331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539477815	chr6:44881371-44881372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572995930	chr6:44881409-44881410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44859200-44889400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr6:44862600-44889400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr6:44864800-44888400	Weak transcription	Primary T cells from cord blood	blood
4	chr6:44873200-44888000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr6:44874800-44889400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr6:44875000-44888800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr6:44877800-44892800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:44879000-44888000	Weak transcription	HepG2	liver
9	chr6:44880600-44888000	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr6:44881000-44881200	Enhancers	Fetal Intestine Small	intestine
11	chr6:44881000-44894600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:44881200-44882200	Weak transcription	Fetal Intestine Small	intestine
13	chr6:44882000-44882800	Enhancers	Fetal Intestine Large	intestine
14	chr6:44882200-44882600	Enhancers	Fetal Intestine Small	intestine
15	chr6:44882400-44886400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:44883800-44886400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:44885000-44885400	Enhancers	Fetal Heart	heart
18	chr6:44885200-44885600	Enhancers	Fetal Stomach	stomach
19	chr6:44885400-44888200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr6:44885400-44888200	Weak transcription	Fetal Heart	heart
21	chr6:44885600-44899200	Weak transcription	Fetal Stomach	stomach
22	chr6:44886400-44886600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:44886400-44886600	Enhancers	NHDF-Ad	bronchial
24	chr6:44886400-44886800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:44886600-44887000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:44886600-44887000	Active TSS	Fetal Lung	lung
27	chr6:44886600-44887000	Flanking Active TSS	NHDF-Ad	bronchial
28	chr6:44886800-44887000	Enhancers	Duodenum Mucosa	Duodenum
29	chr6:44886800-44887200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:44886800-44888600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:44887000-44888600	Weak transcription	Duodenum Mucosa	Duodenum
32	chr6:44887000-44893200	Weak transcription	NHDF-Ad	bronchial
33	chr6:44887400-44887800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr6:44887800-44888200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr6:44888000-44888400	Enhancers	HepG2	liver
36	chr6:44888000-44889000	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr6:44888000-44889200	Enhancers	K562	blood
38	chr6:44888000-44890200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:44888000-44893000	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr6:44888000-44893800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr6:44888000-44896200	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr6:44888200-44888600	Enhancers	Liver	Liver
43	chr6:44888200-44888800	Enhancers	Fetal Heart	heart
44	chr6:44888200-44889200	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr6:44888200-44889600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr6:44888200-44896200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr6:44888400-44889000	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr6:44888400-44889200	Enhancers	NH-A	brain
49	chr6:44888400-44889400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:44888400-44889800	Flanking Active TSS	HepG2	liver

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