Variant report

Variant	nsv606673
Chromosome Location	chr7:38395429-38403455
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	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
2	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
3	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
4	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
5	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
7	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
9	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
10	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
11	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
12	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
13	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
14	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
16	CHD1	chr7:38402581-38402583	GM12878	blood:	n/a	n/a
17	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a
18	CHD2	chr7:38403060-38403224	GM12878	blood:	n/a	n/a
19	CTCF	chr7:38403120-38403270	HCPEpiC	choroid plexus:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
20	CTCF	chr7:38403020-38403170	GM12869	blood:	n/a	n/a
21	CTCF	chr7:38403160-38403310	WI-38	lung:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
22	CTCF	chr7:38399020-38399170	GM12864	blood:	n/a	n/a
23	CTCF	chr7:38398660-38398810	GM12870	blood:	n/a	n/a
24	CTCF	chr7:38398680-38398830	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr7:38399094-38399099	Gliobla	brain:	n/a	n/a
26	CTCF	chr7:38398703-38399012	GM10248	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
27	CTCF	chr7:38399020-38399170	GM12872	blood:	n/a	n/a
28	CTCF	chr7:38399060-38399210	RPTEC	kidney:	n/a	n/a
29	CTCF	chr7:38402440-38402590	GM12875	blood:	n/a	n/a
30	CTCF	chr7:38398657-38398944	A549	lung:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
31	CTCF	chr7:38403020-38403294	ECC-1	luminal epithelium:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
32	CTCF	chr7:38403077-38403336	MCF-7	breast:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
33	CTCF	chr7:38403060-38403342	ProgFib	skin:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
34	CTCF	chr7:38398716-38399000	MCF-7	breast:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
35	CTCF	chr7:38398680-38398830	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr7:38398680-38398830	GM12872	blood:	n/a	n/a
37	CTCF	chr7:38403000-38403150	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr7:38403120-38403270	K562	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
39	CTCF	chr7:38398680-38398830	RPTEC	kidney:	n/a	n/a
40	CTCF	chr7:38403100-38403250	HEK293	kidney:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
41	CTCF	chr7:38403060-38403210	GM12870	blood:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
42	CTCF	chr7:38403082-38403334	Medullo	brain:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
43	CTCF	chr7:38403140-38403290	HepG2	liver:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
44	CTCF	chr7:38403120-38403270	AoAF	blood vessel:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
45	CTCF	chr7:38398660-38398810	HL-60	blood:	n/a	n/a
46	CTCF	chr7:38403160-38403310	HAc	cerebellar:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
47	CTCF	chr7:38398680-38398830	GM12874	blood:	n/a	n/a
48	CTCF	chr7:38403140-38403290	AG09319	gingival:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
49	CTCF	chr7:38399060-38399210	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr7:38402830-38403539	SK-N-SH	brain:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38398836-38398886	U87	brain:	n/a
2	chr7:38398836-38398886	AG09319	gingival:	n/a
3	chr7:38398836-38398886	AoSMC	blood vessel:	n/a
4	chr7:38398836-38398886	A549	lung:	n/a
5	chr7:38398839-38398889	HCPEpiC	choroid plexus:	n/a
6	chr7:38398836-38398886	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:38398836-38398886	HAEpiC	amniotic membrane:	n/a
8	chr7:38398836-38398886	BE2_C	brain:	n/a
9	chr7:38398839-38398889	GM12892	blood:	n/a
10	chr7:38398839-38398889	SKMC	muscle:	n/a
11	chr7:38398836-38398886	AG04450	lung:	fetal
12	chr7:38398836-38398886	HMEC	breast:	n/a
13	chr7:38398836-38398886	SK-N-SH_RA	brain:	n/a
14	chr7:38398836-38398886	SKMC	muscle:	n/a
15	chr7:38398839-38398889	PANC-1	pancreas:	n/a
16	chr7:38398839-38398889	HepG2	liver:	n/a
17	chr7:38398839-38398889	ECC-1	luminal epithelium:	n/a
18	chr7:38398839-38398889	MCF-7	breast:	n/a
19	chr7:38398839-38398889	AG09319	gingival:	n/a
20	chr7:38398839-38398889	Jurkat	blood:	n/a
21	chr7:38398839-38398889	H1-hESC	embryonic stem cell:	embryo
22	chr7:38398839-38398889	BJ	skin:	n/a
23	chr7:38398839-38398889	AG04450	lung:	fetal
24	chr7:38398836-38398886	MCF-7	breast:	n/a
25	chr7:38398839-38398889	ProgFib	skin:	n/a
26	chr7:38398836-38398886	AG04449	skin:	fetal
27	chr7:38398836-38398886	K562	blood:	n/a
28	chr7:38398839-38398889	HRE	kidney:	n/a
29	chr7:38398839-38398889	MCF10A-Er-Src	breast:	n/a
30	chr7:38398839-38398889	SK-N-MC	brain:	n/a
31	chr7:38398836-38398886	BJ	skin:	n/a
32	chr7:38398836-38398886	HCM	heart:	n/a
33	chr7:38398836-38398886	HEEpiC	esophagus:	n/a
34	chr7:38398836-38398886	NH-A	brain:	n/a
35	chr7:38398839-38398889	GM19239	blood:	n/a
36	chr7:38398836-38398886	NHBE	bronchial:	n/a
37	chr7:38398839-38398889	GM06990	blood:	n/a
38	chr7:38398839-38398889	K562	blood:	n/a
39	chr7:38398839-38398889	PFSK-1	brain:	n/a
40	chr7:38398839-38398889	HNPCEpiC	eye:	n/a
41	chr7:38398839-38398889	HIPEpiC	eye:	n/a
42	chr7:38398839-38398889	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:38398836-38398886	HCT-116	colon:	n/a
44	chr7:38398839-38398889	HCM	heart:	n/a
45	chr7:38398836-38398886	LNCaP	prostate:	n/a
46	chr7:38398839-38398889	SK-N-SH_RA	brain:	n/a
47	chr7:38398839-38398889	HL-60	blood:	n/a
48	chr7:38398836-38398886	HL-60	blood:	n/a
49	chr7:38398836-38398886	RPTEC	kidney:	n/a
50	chr7:38398839-38398889	LNCaP	prostate:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
2	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
3	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183

Variant related genes	Relation type
TRGV4	TF binding region
TRGV3	TF binding region
TRGV2	TF binding region
TRGV4	CpG island
TRGV3	CpG island
TRGV2	CpG island

Extended variants
information (count: 604 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:604 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2735128	chr7:38395429-38395430	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs113207615	chr7:38395449-38395450	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs375776220	chr7:38395461-38395462	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs545826742	chr7:38395477-38395478	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75377256	chr7:38395484-38395485	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs148935821	chr7:38395491-38395492	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs548099332	chr7:38395513-38395514	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567878301	chr7:38395546-38395547	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145881651	chr7:38395557-38395558	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
10	rs527519111	chr7:38395561-38395562	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546668285	chr7:38395576-38395577	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566671076	chr7:38395594-38395595	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138498268	chr7:38395595-38395596	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56722594	chr7:38395596-38395597	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558865695	chr7:38395600-38395601	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547763587	chr7:38395604-38395605	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372426613	chr7:38395606-38395607	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538496295	chr7:38395615-38395616	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs193131557	chr7:38395617-38395618	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145131739	chr7:38395641-38395642	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
21	rs369749044	chr7:38395700-38395701	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113900740	chr7:38395727-38395728	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113652752	chr7:38395731-38395732	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369982640	chr7:38395736-38395737	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576828215	chr7:38395737-38395738	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78664884	chr7:38395749-38395750	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150752929	chr7:38395786-38395787	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562479150	chr7:38395802-38395803	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34207156	chr7:38395844-38395845	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531226195	chr7:38395848-38395849	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541707894	chr7:38395865-38395866	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558621584	chr7:38395895-38395896	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543327664	chr7:38395907-38395908	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs137890986	chr7:38395928-38395929	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182754106	chr7:38395934-38395935	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111411110	chr7:38395953-38395954	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76083621	chr7:38395979-38395980	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532610519	chr7:38395980-38395981	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112023190	chr7:38395993-38395994	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552406132	chr7:38395996-38395997	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569219992	chr7:38396008-38396009	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78773647	chr7:38396012-38396013	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148385511	chr7:38396020-38396021	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76675839	chr7:38396030-38396031	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78334174	chr7:38396037-38396038	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143462814	chr7:38396045-38396046	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576967536	chr7:38396048-38396049	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554356929	chr7:38396055-38396056	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577392008	chr7:38396082-38396083	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187460245	chr7:38396178-38396179	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
2	chr7:38389600-38413800	Weak transcription	K562	blood
3	chr7:38391400-38396600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr7:38392400-38398200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:38393600-38395800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr7:38393800-38396000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr7:38393800-38396200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr7:38393800-38398000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr7:38394000-38395600	Enhancers	Primary T cells fromperipheralblood	blood
10	chr7:38394000-38396400	Weak transcription	Primary T cells from cord blood	blood
11	chr7:38394000-38397000	Weak transcription	Primary B cells from cord blood	blood
12	chr7:38394000-38397400	Weak transcription	Thymus	Thymus
13	chr7:38394200-38396200	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr7:38394200-38397600	Weak transcription	Primary B cells from peripheral blood	blood
15	chr7:38394400-38395600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr7:38394400-38396200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr7:38394400-38396600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:38394400-38397000	Enhancers	Dnd41	blood
19	chr7:38394400-38397800	Weak transcription	GM12878-XiMat	blood
20	chr7:38394400-38398200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr7:38394400-38402200	Weak transcription	Spleen	Spleen
22	chr7:38394600-38397600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr7:38395000-38395600	Enhancers	Fetal Thymus	thymus
24	chr7:38395000-38398200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr7:38395000-38400000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:38395200-38398200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:38395400-38396200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr7:38395400-38396400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr7:38395600-38396400	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr7:38395600-38396600	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:38395600-38397800	Weak transcription	Fetal Thymus	thymus
32	chr7:38395800-38397400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:38396000-38397800	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr7:38396200-38396800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr7:38396200-38397200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr7:38396200-38397600	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr7:38396200-38397800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr7:38396400-38396600	Enhancers	Primary T cells from cord blood	blood
39	chr7:38396400-38398000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr7:38396400-38398200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr7:38396600-38396800	Enhancers	Fetal Stomach	stomach
42	chr7:38396600-38397000	Active TSS	Primary T cells from cord blood	blood
43	chr7:38396600-38397200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr7:38396600-38397200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr7:38396600-38397600	Enhancers	Primary T cells fromperipheralblood	blood
46	chr7:38396800-38397800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr7:38396800-38398000	Weak transcription	Fetal Stomach	stomach
48	chr7:38397000-38397200	Enhancers	Primary B cells from cord blood	blood
49	chr7:38397000-38397200	Flanking Active TSS	Primary T cells from cord blood	blood
50	chr7:38397000-38397200	Flanking Active TSS	Dnd41	blood

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